참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Pyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]- | HCID 12449554 | — |
| 반응물 | Piperidin-3-amine dihydrochloride | HCID 16211870 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | HCID 131730771 | HCID 131730771 | 27.5% |
반응 단계
3-Chloro-6-(4-trifluoromethylphenyl)pyridazine (0.2 g, 0.77 mmol), 3-aminopiperidine dihydrochloride (0.27 g, 1.54 mmol) and potassium carbonate (0.53 g, 3.87 mmol) were mixed in acetone (4 mL) in a 20 mL microwave vessel. The reaction mixture was heated in a microwave oven for 2 h at 120° C. The reaction mixture was filtered and the precipitate was washed with MeOH. The combined organic phases were evaporated. The crude oil was purified on a silicagel column (0.04-0.063 mesh) using dichloromethane/MeOH (9:1) as eluent. This afforded 110 mg of a oil that was dissolved in MeOH and acidified with concentrated HCl (5 mL). The mixture was evaporated and the residue was dissolved in MeOH (1 mL) and ether (100 mL) was added with stirring. The mixture was evaporated to give 76 mg (25%) of the title compound as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846677B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-fee32dfc11fb4f769ef6a6273104e86b |
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| 출처 메모 | uspto-grants-2014_09 |
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